Answer:
The correct answer is option a. "Plasmodial slime mold".
Explanation:
Plasmodial slime molds, are comprised of a single "supercell" with thousands or millions of nuclei within it. These organisms are formed by the fusion of multiple flagellated cells. The formation of these single celled organisms depend on the presence of enough food source. Typically, plasmodial slime molds have a diameter of 3 to 4 centimeters, but they can growth up to 30 centimeters.
structure of a compound influences its function in many ways like we take example of phospholipid bilayer 1. The fact that the tails are hydrophobic means that they do not interact with water. When a bunch of phospholipids are floating around in water, they try to arrange themselves in a bilayer that shields the hydrophobic parts from water-based, or aqueous, surroundings.
2. The heads are hydrophilic and can then interact with water and other polar or charged substances on either side of the bilayer. The bilayer acts as a barrier that allows cells to maintain internal conditions that are different from external conditions, which is monumentally important for cells to operate properly.
3. Phospholipids demonstrate the intersection of structure and function in another way, too. We already know that fatty acids can be saturated or unsaturated and that unsaturated fatty acids have bends in their chains. Those bends prevent fatty acids from packing close.
The correct answer is a. with; diffusion
Im not really sure , but it might have something to do with polar chemical compound <span />
If a scientist wanted to compare the expression of one gene under two sets of conditions, chain termination is the technique they would use.
Chain termination is any chemical response that ceases the formation of reactive intermediates in a sequence propagation step withinside the route of a polymerization, efficaciously bringing it to a halt.
Sanger sequencing, additionally referred to as the “chain termination technique”, is a way for figuring out the nucleotide collection of DNA. The approach become evolved with the aid of using time Nobel Laureate Frederick Sanger and his colleagues in 1977, subsequently the call the Sanger Sequence.
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